慢性便秘和肠易激综合征与消化道癌症的因果关系:孟德尔随机研究

Rencai Fan, Jiaqi Zhang, Jiaofeng Shen, Chenkai Mao, Shicheng Li, Zhixiang Zhuang
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引用次数: 0

摘要

背景:慢性便秘和肠易激综合征(IBS)是普遍存在的胃肠道疾病,而消化道癌症(DTC)则是全球福祉面临的严峻挑战。然而,现有的观察性研究对便秘和肠易激综合征与 DTCs 易感性的潜在因果关系提供了不确定的见解:我们进行了孟德尔随机化(MR)分析,以确定这些症状与七类不同的 DTCs 之间的因果关系,包括结直肠癌(CRC)、肝细胞癌(HCC)、食管恶性肿瘤(ESCA)、胰腺腺癌(PAAD)、胆道癌(BTCs)、胃癌(GC)和小肠肿瘤(SIC)。利用从 FinnGen 数据库的 GWAS 数据中获得的工具变量(IVs),我们采用了一系列分析方法,包括逆方差加权乘法随机效应(IVW_MRE)、逆方差加权固定效应(IVW_FE)、最大似然法(ML)、加权中位数(WM)、MR-Egger 回归和 MR-PRESSO 检验:通过 IVW 方法,我们观察到遗传预测便秘与 PAAD 易感性增加之间存在实质性联系(OR = 2.29,95% CI:1.422-3.69,P = 0.001)。通过 MR-PRESSO 去除离群 SNP 后,遗传预测的肠易激综合征与 CRC 风险增加有关(OR = 1.17,95% CI:1-1.37,P = 0.05)。尽管如此,便秘或肠易激综合征与其他 DTCs 的决定性因果关系仍然难以捉摸:总之,在欧洲队列中,遗传学预测的便秘与 PAAD 风险增加有关,而肠易激综合征与 CRC 易感性增加有关,这与一些观察性研究一致。然而,便秘和肠易激综合征与其他 DTCs 的因果关系仍未确定。
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Causal Relationships of Chronic Constipation and Irritable Bowel Syndrome with Digestive Tract Cancers: A Mendelian Randomization Study.

Background: Chronic constipation and irritable bowel syndrome (IBS) manifest as prevalent gastrointestinal disorders, while digestive tract cancers (DTCs) present formidable challenges to global well-being. However, extant observational studies proffer uncertain insights into potential causal relationships of constipation and IBS with susceptibility to DTCs.

Methods: We executed Mendelian randomization (MR) analysis to establish causal connections between these conditions and seven distinct categories of DTCs, including colorectal carcinoma (CRC), hepatocellular cancer (HCC), esophageal malignancy (ESCA), pancreatic adenocarcinoma (PAAD), biliary tract carcinoma (BTCs), gastric carcinoma (GC), and small intestine neoplasm (SIC). Leveraging instrumental variables (IVs) obtained from GWAS data of the FinnGen database, we employed a range of analytical methodologies, including inverse-variance weighting multiplicative random effects (IVW_MRE), inverse-variance weighting fixed effects (IVW_FE), maximum likelihood (ML), weighted median (WM), MR‒Egger regression, and the MR-PRESSO test.

Results: We observed a substantial linkage between genetically predicted constipation and increased vulnerability to PAAD (OR = 2.29, 95% CI: 1.422-3.69, P = 0.001) via the IVW method. Following the removal of outlier SNPs through MR-PRESSO, genetically predicted IBS was affiliated with an increased risk of CRC (OR = 1.17, 95% CI: 1-1.37, P = 0.05). Nonetheless, decisive causal correlations of constipation or IBS with other DTCs remain elusive.

Conclusion: In summary, genetically predicted constipation was associated with an augmented PAAD risk, and IBS was associated with an increased CRC susceptibility within European cohorts, in agreement with some observational studies. Nevertheless, the causal associations of constipation and IBS with other DTCs remain inconclusive.

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